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Revision as of 17:13, 10 April 2011
Not to be confused with xanthine.This article does not cite any sources. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. Find sources: "Xanthene" – news · newspapers · books · scholar · JSTOR (December 2009) (Learn how and when to remove this message) |
Names | |
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IUPAC name 9H-Xanthene | |
Other names
Dibenzopyran 10H-9-oxaanthracene | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ECHA InfoCard | 100.001.996 |
EC Number |
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CompTox Dashboard (EPA) | |
SMILES
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Properties | |
Chemical formula | Template:Carbon13Template:Hydrogen10Template:Oxygen |
Molar mass | 182.22 g/mol |
Appearance | Yellow solid |
Melting point | 101-102 °C |
Boiling point | 310-312 °C |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
Xanthene (9H-xanthene, 10H-9-oxaanthracene) is a yellow organic heterocyclic compound. Its chemical formula is Template:Carbon13Template:Hydrogen10Template:Oxygen. It is soluble in diethyl ether. Its melting point is 101-102 °C and its boiling point is 310-312 °C. Xanthene is used as a fungicide and it is also a useful intermediate in organic synthesis.
Derivatives of xanthene are commonly referred to collectively as xanthenes, and among other uses are the basis of a class of dyes which includes fluorescein, eosins, and rhodamines. Xanthene dyes tend to be fluorescent, yellow to pink to bluish red, brilliant dyes. Many xanthene dyes can be prepared by condensation of derivates of phthalic anhydride with derivates of resorcinol or 3-aminophenol.
See also
- Xanthone
- Xanthene
- Xanthydrol
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